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CCTTAAACTTCCCCTGTCCCTTACC[A/G]GCAGCCTCCTGCTCCGGAAGTTTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616804 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
VSTM1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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VSTM1 - V-set and transmembrane domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001288791.1 | 1035 | Silent Mutation | GCC,GCT | A,A 96 | NP_001275720.1 | |
NM_001288792.1 | 1035 | Silent Mutation | GCC,GCT | A,A 153 | NP_001275721.1 | |
NM_001288793.1 | 1035 | Silent Mutation | GCC,GCT | A,A 64 | NP_001275722.1 | |
NM_198481.3 | 1035 | Silent Mutation | GCC,GCT | A,A 184 | NP_940883.2 | |
XM_011526845.1 | 1035 | Silent Mutation | GCC,GCT | A,A 312 | XP_011525147.1 | |
XM_011526846.1 | 1035 | Silent Mutation | GCC,GCT | A,A 282 | XP_011525148.1 | |
XM_011526847.1 | 1035 | Missense Mutation | CCG,CTG | P,L 305 | XP_011525149.1 | |
XM_011526848.1 | 1035 | Silent Mutation | GCC,GCT | A,A 251 | XP_011525150.1 | |
XM_011526849.1 | 1035 | Silent Mutation | GCC,GCT | A,A 214 | XP_011525151.1 | |
XM_017026666.1 | 1035 | UTR 3 | XP_016882155.1 |